Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP636546.RAkUgVWMBxeFoRa88G0HbS6E6e36r1YeUKZ0EaWdSSLec130_assertion> ?p ?o ?g. }
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- NP636546.RAkUgVWMBxeFoRa88G0HbS6E6e36r1YeUKZ0EaWdSSLec130_assertion type Assertion NP636546.RAkUgVWMBxeFoRa88G0HbS6E6e36r1YeUKZ0EaWdSSLec130_head.
- NP636546.RAkUgVWMBxeFoRa88G0HbS6E6e36r1YeUKZ0EaWdSSLec130_assertion description "[Microcephalic osteodysplastic primordial dwarfism type II (MOPD II, MIM 210720) and Seckel syndrome (SCKL, MIM 210600) belong to the primordial dwarfism group characterised by intrauterine growth retardation, severe proportionate short stature, and pronounced microcephaly.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP636546.RAkUgVWMBxeFoRa88G0HbS6E6e36r1YeUKZ0EaWdSSLec130_provenance.
- NP636546.RAkUgVWMBxeFoRa88G0HbS6E6e36r1YeUKZ0EaWdSSLec130_assertion evidence source_evidence_literature NP636546.RAkUgVWMBxeFoRa88G0HbS6E6e36r1YeUKZ0EaWdSSLec130_provenance.
- NP636546.RAkUgVWMBxeFoRa88G0HbS6E6e36r1YeUKZ0EaWdSSLec130_assertion SIO_000772 19643772 NP636546.RAkUgVWMBxeFoRa88G0HbS6E6e36r1YeUKZ0EaWdSSLec130_provenance.
- NP636546.RAkUgVWMBxeFoRa88G0HbS6E6e36r1YeUKZ0EaWdSSLec130_assertion wasDerivedFrom befree-20140225 NP636546.RAkUgVWMBxeFoRa88G0HbS6E6e36r1YeUKZ0EaWdSSLec130_provenance.
- NP636546.RAkUgVWMBxeFoRa88G0HbS6E6e36r1YeUKZ0EaWdSSLec130_assertion wasGeneratedBy ECO_0000203 NP636546.RAkUgVWMBxeFoRa88G0HbS6E6e36r1YeUKZ0EaWdSSLec130_provenance.